Canonical Allele Identifier: PA141321
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47548
ClinVar RCV Id: RCV000040817 RCV000172188 RCV000268106 RCV000272165 RCV000325497 RCV000360898 RCV000382966 RCV001083436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala31693Asp
CA141318
NM_001267550.2:c.95078C>A